Misys Laboratory System , Versions 5.2, 5.23 and 5.3
FDA device recall Z-0631-03 · posted 2003-03-12 · Terminated
Recall details
- Recalling firm
- Misys Healthcare Systems
- Reason for recall
- Missing patient data on Location Chart Copy Cumulative Reports.
- Action taken
- Recall notice was faxed to customers on 2/7/2003. A software correction will be developed and another notice will be made that this is available.
- Root cause
- Other
- Status
- Terminated
- Product code
- JQP
- Quantity affected
- 478
- Distribution
- Nationwide and to Bermuda, Canada, United Kingdom, Ireland, Denmark, Saudi Arabia, United Arab Emirates.
- Date initiated
- 2003-02-07
- Date posted
- 2003-03-12
- Date terminated
- 2004-06-02
- Location
- Tucson, AZ
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